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Helene Reichel

Publications and source records attributed to Helene Reichel.

2 recordsLinked to original sources

Controlling catalyst agglomeration in high-density unordered III-V nanowire growth using Au colloid solutions

III-V semiconductor nanowires (NWs) are a promising platform for optoelectronic and photoelectrochemical applications, where device performance strongly depends on NW density and spatial arrangement. While ordered arrays provide precise control, their fabrication requires complex and costly lithographic techniques. Unordered growth offers a scalable alternative but is limited by insufficient control over catalyst distribution and particle agglomeration. Here, we investigate the density scaling of unordered III-V NW arrays using commercially available Au colloid solutions as catalysts for NW growth via vapor-liquid-solid growth mode. Repeated deposition cycles yield a near-linear increase in particle density, which is ultimately limited by non-linear agglomeration effects not captured by simple stochastic models. To address this limitation, a previously established pre-anneal growth concept is transferred from patterned catalyst arrays to randomly deposited Au colloids, thereby suppressing thermally induced coalescence and stabilizing the catalyst distribution. This approach enables up to a tenfold increase in NW density while improving uniformity and vertical yield. The method is demonstrated for colloid diameters between 100 and 200 nm. Overall, this work provides a scalable, lithography-free route toward high-density III-V NW ensembles and offers insight into the role of particle dynamics in colloid-based growth processes.

cond-mat.mtrl-sci

Tailoring the Nucleation and Growth of Silver Nanoparticles by Sputtering Deposition under Acoustic Wave Activation. Assessment of Plasma Conditions and 2D Patterning Phenomena

Early results on the plasma deposition of dielectric thin films on acoustic wave (AW) activated substrates revealed a densification pattern arisen from the focusing of plasma ions and their impact on specific areas of the piezoelectric substrate. Herein, we extend this methodology to tailor the plasma deposition of metals onto AW-activated LiNbO3 piezoelectric substrates. Our investigation reveals the tracking of the initial stages of nanoparticle (NP) formation and growth during the submonolayer deposition of silver. We elucidate the specific role of AW activation in reducing particle size, enhancing particle circularity, and retarding NP agglomeration and account for the physical phenomena making these processes differ from those occurring on non-activated substrates. We provide a comparative analysis of the results obtained under two representative plasma conditions: diode DC sputtering and magnetron sputtering. In the latter case, the AW activation gives rise to a 2D pattern of domains with different amounts of silver and a distinct size and circularity for the silver NPs. This difference was attributed to the specific characteristics of the plasma sheath formed onto the substrate in each case. The possibilities of tuning the plasmon resonance absorption of silver NPs by AW activation of the sputtering deposition process are discussed.

physics.app-ph